Evidence map›Paper›PMID 32213735›Full record

ArticleThe Journal of reproduction and development2020

Developmental competence of interspecies cloned embryos produced using cells from large Japanese field mice (Apodemus speciosus) and oocytes from laboratory mice (Mus musculus domesticus).

Rika Azuma, Yuki Hatanaka, Seung-Wook Shin, Hitoshi Murai, Minoru Miyashita, Masayuki Anzai, Kazuya Matsumoto

Open access · goldAbstract read
In one paragraph

Article in The Journal of reproduction and development, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 2 countries.

Rika AzumaGraduate School of Biology-Oriented Science and Technology, Kindai University, Wakayama 649-6493, Japan.
Yuki HatanakaMRC Clinical Sciences Centre, Imperial College Faculty of Medicine, W12 0NN London, UK.
Seung-Wook ShinLaboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Maryland 20892, USA.
Hitoshi MuraiToyama Municipal Family Park Zoo Co., Ltd., Toyama 930-0151, Japan.
Minoru MiyashitaFoundation Ube Tokiwa Zoological Society, Yamaguchi 755-0001, Japan.
Masayuki AnzaiGraduate School of Biology-Oriented Science and Technology, Kindai University, Wakayama 649-6493, Japan.
Kazuya MatsumotoGraduate School of Biology-Oriented Science and Technology, Kindai University, Wakayama 649-6493, Japan.
Kindai University · JPNational Institutes of Health · USRIKEN BioResource Research Center · JPTokiwa Park · JPToyama Science Museum · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The large Japanese field mouse (Apodemus speciosus) is endemic to Japan and may be used as an animal model for studies related to environmental pollution, medical science, and basic biology. However, the large Japanese field mouse has low reproductive ability due to the small number of oocytes ovulated per female. To produce experimental models, we investigated the in vitro developmental potential of interspecies somatic cell nuclear transfer (iSCNT) embryos produced by fusing tail tip cells from the large Japanese field mouse with enucleated oocytes from laboratory mice (Mus musculus domesticus). Only a small number of iSCNT embryos developed to the 4-cell (0-4%) and blastocysts (0-1%) stages under sequential treatment using trichostatin A (TSA) and vitamin C (VC) supplemented with deionized bovine serum albumin (d-BSA). This sequential treatment led to the reduction in H3K9 trimethylation and did not affect H3K4 trimethylation in at least the 2-cell stage of the iSCNT embryos. Moreover, iSCNT embryos that received tail tip cells with exposure treatment to ooplasm from cell fusion to oocyte activation or VC treatment prior to cell fusion did not exhibit significant in vitro development improvement compared to that of each control group. This suggests that large Japanese field mice/laboratory mice iSCNT embryos that received sequential treatment using TSA and VC with d-BSA may have slightly better developmental potential beyond the 4-cell stage. Our results provide insights into the reprogramming barriers impeding the wider implementation of iSCNT technology.

Indexed as

Nuclear Transfer TechniquesAnimalsCloning, OrganismEmbryo, MammalianEmbryonic DevelopmentFemaleMiceMurinaeOocytesEpigeneticsGenetic resourceInterspecies somatic cell nuclear transferLarge Japanese field mouseReprogramming

Identifiers

PMID32213735
PMCPMC7297636
OpenAlexW3013378109

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.